Yellow nail syndrome : not a genetic disorder? Eleven new cases and a review of the literature
Identifieur interne : 000473 ( PascalFrancis/Corpus ); précédent : 000472; suivant : 000474Yellow nail syndrome : not a genetic disorder? Eleven new cases and a review of the literature
Auteurs : S. R. Hoque ; S. Mansour ; P. S. MortimerSource :
- British journal of dermatology : (1951) [ 0007-0963 ] ; 2007.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Background Yellow nail syndrome (YNS) is characterized by the triad of characteristic nail changes, chronic respiratory disorders and primary lymphoedema. Over 100 cases have been published, most of which have been sporadic. Despite this, YNS is classified as a dominantly inherited lymphoedema with variable expression. There have been only a few published reports where a positive family history (FH) has been documented in cases of YNS. Objectives To conduct a retrospective survey investigating the genetic basis of YNS. Methods The notes of 11 patients diagnosed with YNS were examined for documentation of a positive FH, and in addition a postal questionnaire was sent to these patients. Results Only one of the 11 patients had a relevant FH. In addition, four patients had complete recovery of their nail changes. Conclusions This is the first retrospective study of YNS to document clear remission of nail changes. The lack of a positive FH in the majority of patients in our study, the late onset of the disease and recovery of nail changes in our patients suggest that YNS may not be primarily a genetic disease as it is currently classified.
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Format Inist (serveur)
NO : | PASCAL 07-0273501 INIST |
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ET : | Yellow nail syndrome : not a genetic disorder? Eleven new cases and a review of the literature |
AU : | HOQUE (S. R.); MANSOUR (S.); MORTIMER (P. S.) |
AF : | Department of Dermatology, St Helier Hospital/Carshalton, Surrey SM5 1AA/Royaume-Uni (1 aut.); SW Thames Regional Genetics Unit, St George's Hospital, University of London/London SW17 0RE/Royaume-Uni (2 aut.); Dermatology Unit, Cardiac and Vascular Sciences, St George's Hospital, University of London/London SW17 0RE/Royaume-Uni (3 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | British journal of dermatology : (1951); ISSN 0007-0963; Coden BJDEAZ; Royaume-Uni; Da. 2007; Vol. 156; No. 6; Pp. 1230-1234; Bibl. 24 ref. |
LA : | Anglais |
EA : | Background Yellow nail syndrome (YNS) is characterized by the triad of characteristic nail changes, chronic respiratory disorders and primary lymphoedema. Over 100 cases have been published, most of which have been sporadic. Despite this, YNS is classified as a dominantly inherited lymphoedema with variable expression. There have been only a few published reports where a positive family history (FH) has been documented in cases of YNS. Objectives To conduct a retrospective survey investigating the genetic basis of YNS. Methods The notes of 11 patients diagnosed with YNS were examined for documentation of a positive FH, and in addition a postal questionnaire was sent to these patients. Results Only one of the 11 patients had a relevant FH. In addition, four patients had complete recovery of their nail changes. Conclusions This is the first retrospective study of YNS to document clear remission of nail changes. The lack of a positive FH in the majority of patients in our study, the late onset of the disease and recovery of nail changes in our patients suggest that YNS may not be primarily a genetic disease as it is currently classified. |
CC : | 002B08H; 002B12B04 |
FD : | Ongle jaune syndrome; Lymphoedème; Génétique; Désordre; Article synthèse; Dermatologie |
FG : | Peau pathologie; Appareil circulatoire pathologie; Lymphatique pathologie |
ED : | Yellow nail syndrome; Lymphedema; Genetics; Disorder; Review; Dermatology |
EG : | Skin disease; Cardiovascular disease; Lymphatic vessel disease |
SD : | Uña amarilla síndrome; Linfedema; Genética; Desorden; Artículo síntesis; Dermatología |
LO : | INIST-1043.354000149620140120 |
ID : | 07-0273501 |
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Pascal:07-0273501Le document en format XML
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<front><div type="abstract" xml:lang="en">Background Yellow nail syndrome (YNS) is characterized by the triad of characteristic nail changes, chronic respiratory disorders and primary lymphoedema. Over 100 cases have been published, most of which have been sporadic. Despite this, YNS is classified as a dominantly inherited lymphoedema with variable expression. There have been only a few published reports where a positive family history (FH) has been documented in cases of YNS. Objectives To conduct a retrospective survey investigating the genetic basis of YNS. Methods The notes of 11 patients diagnosed with YNS were examined for documentation of a positive FH, and in addition a postal questionnaire was sent to these patients. Results Only one of the 11 patients had a relevant FH. In addition, four patients had complete recovery of their nail changes. Conclusions This is the first retrospective study of YNS to document clear remission of nail changes. The lack of a positive FH in the majority of patients in our study, the late onset of the disease and recovery of nail changes in our patients suggest that YNS may not be primarily a genetic disease as it is currently classified.</div>
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<ET>Yellow nail syndrome : not a genetic disorder? Eleven new cases and a review of the literature</ET>
<AU>HOQUE (S. R.); MANSOUR (S.); MORTIMER (P. S.)</AU>
<AF>Department of Dermatology, St Helier Hospital/Carshalton, Surrey SM5 1AA/Royaume-Uni (1 aut.); SW Thames Regional Genetics Unit, St George's Hospital, University of London/London SW17 0RE/Royaume-Uni (2 aut.); Dermatology Unit, Cardiac and Vascular Sciences, St George's Hospital, University of London/London SW17 0RE/Royaume-Uni (3 aut.)</AF>
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<EA>Background Yellow nail syndrome (YNS) is characterized by the triad of characteristic nail changes, chronic respiratory disorders and primary lymphoedema. Over 100 cases have been published, most of which have been sporadic. Despite this, YNS is classified as a dominantly inherited lymphoedema with variable expression. There have been only a few published reports where a positive family history (FH) has been documented in cases of YNS. Objectives To conduct a retrospective survey investigating the genetic basis of YNS. Methods The notes of 11 patients diagnosed with YNS were examined for documentation of a positive FH, and in addition a postal questionnaire was sent to these patients. Results Only one of the 11 patients had a relevant FH. In addition, four patients had complete recovery of their nail changes. Conclusions This is the first retrospective study of YNS to document clear remission of nail changes. The lack of a positive FH in the majority of patients in our study, the late onset of the disease and recovery of nail changes in our patients suggest that YNS may not be primarily a genetic disease as it is currently classified.</EA>
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